Identity
- Trade Name
- Surgical Direct FDA UDI
- Generic Name
- Eye muscle hook, reusable FDA UDI
- Device Name
- 9 1/2 inch Kirschner Bow , Extra-Large FDA UDI
- Model / Reference
- SD914221103 FDA UDI
- Description
- 9 1/2 inch Kirschner Bow , Extra-Large FDA UDI
Identifiers
- Catalog Number
- SD914221103 FDA UDI
- Primary DI / UDI-DI
- B382SD9142211030 FDA UDI
- FDA Product Code
- FGN FDA UDI
- GMDN Term
- Eye muscle hook, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4730 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Eye muscle hook, reusable
Surgical Direct by Surgical Direct, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Ambler Surgical — Ambler Surgical, LLC · Class I
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- Sklar — Sklar Corporation · Class I
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Surgical Direct, Inc.
Sources (1)
- FDA UDI 77cec7bf-ad65-4cf2-95be-587120f6ea62 35 fields · synced May 30, 2026